<<Disclaimer: Verify this information before applying it to your situation.>> Well, nothing like beating a dead horse but.... My 9 1/2 year old daughter had a biopsy a week ago Tuesday at Columbia Presbyterian by Dr. Peter Green. As many of you know, he is one of the top celiac guys in the country and I really respect and like this guy. I mention this only because I want it understood that this biopsy was read by the best. Well I was expecting a very "black and white" answer,but that is not what I got. Dr. Green called me last night to tell me that there *was* damage to some parts of the intestine but it was not in stricked keeping with celiac. He said he looked that report over for a second time with the pathologist (who he says is the best in the world!) and neither one are willing to say if it is or isn't. He was honestly stumped. So I can either wait and redo her biopsy in 6 months to a year or I can have her go gluten free. I should mention that we do not have classic symptoms. I am newly diagnosed as of May. Our symptoms tend to be constipation, fatigue, short stature, joint pain, gas, bloating and intermittent stomach pain. The only other person in my family who has celiac (so far ) is my brother's child who was diagnosed 3 years ago at age 3. My other daughter had blood work done which came back the same as this daugher in question, with the Antigliadin IgG elevated but the Antigliadin IgA and the Antiendoysium IgA were both negative. So even the bloodwork is inconclusive. I am feeling very frustrated. At one time my daughter had elisa and rast testing and there were "high numbers" next to gluten, casein and milk , I believe. So that is my story. What do you guys think I should do??????????? Yours in good health, Lisa Zafar Orange County, NY